# Intubation with Eagle Syndrome

**URL:** <https://forum.livingwitheagle.org/t/intubation-with-eagle-syndrome/7209>\
**Category:** General\
**Created:** [April 29, 2020, 4:10am UTC](https://forum.livingwitheagle.org/t/intubation-with-eagle-syndrome/7209 "2020-04-29T04:10:26Z")\
**Posts on this page:** 1\
**Showing post:** 2

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**Author:** ![Jules](https://yyz1.discourse-cdn.com/flex027/user_avatar/forum.livingwitheagle.org/jules/32/404_2.png) [@Jules](https://forum.livingwitheagle.org/u/Jules)\
**Post date:** [April 29, 2020, 5:52pm UTC](https://forum.livingwitheagle.org/t/intubation-with-eagle-syndrome/7209/2 "2020-04-29T17:52:02Z")

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Very good idea! I know that several members have been very concerned about this with having the ES & other procedures & have mentioned it to the anaesthetist.  
You might find this article interesting too:

> [@Don’t Get Mad, Get Proactive: A Covid-19 Weapon for YOU](https://forum.livingwitheagle.org/t/don-t-get-mad-get-proactive-a-covid-19-weapon-for-you/7060):
>
> Yes, we have a public health crisis. And as rare disease patients, we are “at risk”. Being marginalized as a rare disease patient is nothing new to us. But this time is different! There are 7000 rare diseases that affect 30 million in America and another 30 million in Europe. Washing our hands, buying toilet paper and hand sanitizer just don’t cut it. Well-intended statements from health and government officials, meant to allay fears in the general population, can increase anxiety in ours. I…

Hope that you don’t get the virus…keep safe as much as you can.

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